Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23868273-23868564 | Common:5; Rare:72; Clinvar:1; Clinvar (benign):4 | ||||
chr1:23959136-23959299 | Common:2; Rare:29 | ||||
chr1:23959599-23959916 | Common:2; Rare:84 | ||||
chr1:24642971-24643335 | Common:2; Rare:113 | ||||
chr1:25232428-25232719 | Rare:108 | ||||
chr1:25247413-25247630 | Common:2; Rare:81 | ||||
chr1:25267913-25268237 | Common:7; Rare:63 | ||||
chr1:25338204-25338447 | Common:1; Rare:86 | ||||
chr1:25819878-25820029 | Common:3; Rare:47 | ||||
chr1:26111737-26111856 | Rare:39 | ||||
chr1:26279908-26280201 | Rare:160 | ||||
chr1:26306620-26306851 | Common:13; Rare:71 | ||||
chr1:26317844-26317997 | Common:2; Rare:19 | ||||
chr1:26432100-26432439 | Common:5; Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472102-26472523 | Common:5; Rare:121 |